Short-Range Disorder in TeO2 Melt and Glass
Author(s) -
Oliver L. G. Alderman,
Chris J. Benmore,
Steve Feller,
E. I. Kamitsos,
E.D. Simandiras,
Dimitrios G. Liakos,
Martha Jesuit,
Makyla Boyd,
Michael Packard,
Richárd Wéber
Publication year - 2019
Publication title -
the journal of physical chemistry letters
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.563
H-Index - 203
ISSN - 1948-7185
DOI - 10.1021/acs.jpclett.9b03231
Subject(s) - cutoff , coordination number , raman spectroscopy , range (aeronautics) , cluster (spacecraft) , distribution (mathematics) , materials science , pair distribution function , oxide , raman scattering , condensed matter physics , molecular physics , atmospheric temperature range , chemical physics , chemistry , thermodynamics , physics , optics , quantum mechanics , mathematics , ion , composite material , mathematical analysis , computer science , metallurgy , programming language
High-resolution X-ray pair distribution functions for molten and glassy TeO 2 reveal coordination numbers n TeO ≈ 4. However, distinct from the known α-, β-, and γ-TeO 2 polymorphs, there is considerable short-range disorder such that no clear cutoff distance between bonded and nonbonded interactions exists. We suggest that this is similar to disorder in δ-TeO 2 and arises from a broad distribution of asymmetric Te-O-Te bridges, something that we observe becomes increasingly asymmetric with increasing liquid temperature. Such behavior is qualitatively consistent with existing interpretations of Raman scattering spectra, and equivalent to temperature-induced coordination number reduction, for sufficiently large cutoff radii. Therefore, TeO 2 contains a distribution of local environments that are, furthermore, temperature dependent, making it distinct from the canonical single-oxide glass formers. Our results are in good agreement with high-level ab initio cluster calculations.
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